FAM53B truncation caused by t(10;19)(q26;q13) chromosome translocation in acute lymphoblastic leukemia

RNA-sequencing of the patient's bone marrow detected fusion transcripts in which the coding sequence of the FAM53B gene (from 10q26) was fused to a genomic sequence (from 19q13) that mapped upstream of the SLC7A10 locus. Reverse transcription-polymerase chain reaction together with Sanger seque...

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Publicat a:Oncol Lett
Autors principals: Panagopoulos, Ioannis, Gorunova, Ludmila, Torkildsen, Synne, Tierens, Anne, Heim, Sverre, Micci, Francesca
Format: Artigo
Idioma:Inglês
Publicat: D.A. Spandidos 2017
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Articles
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5403202/
https://ncbi.nlm.nih.gov/pubmed/28454383
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/ol.2017.5705
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